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632 Possible Causes for Possibly Scoliosis, Prognathism, Tall Stature

Did you mean: Possibly, Scoliosis, Prognathism, Tall Stature

  • Marfan Syndrome

    Vision problems should be treated when possible. Monitor for scoliosis, especially during the teenage years.[] The patient was diagnosed as bilateral temporomandibular joints arthrosis with mandibular prognathism.[] It is characterized by tall stature, elongated extremities, mitral valve prolapse, aortic dilatation, aortic dissection, and sublaxation of the lens A hereditary disorder[]

  • Acromegaly

    He died as a result of pulmonary compromise secondary to advanced scoliosis. Fig. 1.[] Craniofacial soft tissue and skeletal changes including mandibular prognathism and disturbed occlusion are typical manifestations of the disease process.[] Convert to ICD-10-CM : 253.0 converts approximately to: 2015/16 ICD-10-CM E22.0 Acromegaly and pituitary gigantism Approximate Synonyms Acromegaly Constitutional tall stature[]

  • Gigantism

    Voice is hoarse and affected individuals have a plump, stocky body with pectus excavatum, thoracic scoliosis, hepatosplenomegaly, umbilical and/or inguinal hernias, broad[] It appears in childhood and many morphological signs lead us to suspect it: enlarged hands and feet, thick skin, a prominent chin (called prognathism), and an abnormal tendency[] This boy appears likely to have neurofibromatosis type 1 (NF1) which raises the question of subtle GH excess in NF1 patients with tall stature.[]

  • Sotos Syndrome

    Other possible symptoms and signs can include: behavioral disturbances, intellectual disability, scoliosis, seizures, heart defects, kidney defects, weak muscle tone, stuttering[] Oral findings include prognathism and a high-arched palate with premature eruption of the teeth. Delayed psychomotor development increases the risk for caries.[] Constitutional tall stature Tall stature in childhood usually presents less initial concern than short stature because, at least in early childhood, being tall can be advantageous[]

  • Klinefelter Syndrome

    Osteoporosis may lead to vertebral collapse and even scoliosis.[] […] the addition of an extra X to a 47,XXY karyotype A more abnormal phenotype including facial anomalies such as hypertelorism, epicanthic folds, simplified ears, and mild prognathism[] These patients usually present with tall stature. We report a case of KS with short stature due to growth hormone deficiency.[]

  • Gigantism - Acromegaly

    […] development, particularly motor skills such as sitting and crawling.Other signs and symptoms of Sotos syndrome can include an abnormal side-to-side curvature of the spine (scoliosis[] The mandible also characteristically enlarges resulting in prognathism and gaps between the teeth 10 .[] Publisher Full Text Tall stature: a difficult diagnosis?[]

  • Spondyloepimetaphyseal Dysplasia Type SPONASTRIME

    Sponastrime dysplasia is a rare skeletal dysplasia characterized by severe short stature, scoliosis, a saddle nose, frontal bossing, and increased upper/lower segment ratio[] The potential for difficult direct laryngoscopy and tracheal intubation is present because of the large head, abnormal facies, and mild prognathism.[] Pseudodiastrophic dysplasia AR Unknown Spondyloepimetaphyseal dysplasia with joint laxity AR Unknown AD, autosomal dominant; AR, autosomal recessive; CATSHL, camptodactyly, tall[]

  • Launois Syndrome

    […] abnormalities (12 %): patent ductus arteriosus, VSD, coarctation of the aorta, atrial fibrillation skeletal abnormalities: asymmetry (skull, limbs) ipsilateral to the nevus; scoliosis[] Gigantism typifies childhood onset of disease, when epiphyseal plates have not closed, leading to excessive growth of bones and thus an abnormally tall stature.[] stature 2016 2017 2018 2019 Billable/Specific Code Applicable To Constitutional gigantism E34.4 ) constitutional tall stature ( ICD-10-CM Diagnosis Code E34.4 Constitutional[]

  • Autosomal Dominant Prognathism

    In 10 patients, scoliosis was idiopathic.[] Homepage Rare diseases Search Search for a rare disease Autosomal dominant prognathism Disease definition A rare, genetic, developmental defect during embryogenesis disorder[] The same excess of growth hormone in individuals whose epiphyses have not fused will result in gigantism (excessively tall stature).[]

  • Cleidocranial Dysplasia

    […] the spaces between the bones of the skull Underdeveloped cheekbones and prominent brow bone Wide nasal bridge due to increased space between the eyes High arched palate or possible[] […] craniofacial features of CCD that stand out are a patency of the anterior fontanelle, an inverted pear-shaped calvaria, a hypertelorism, a general midface retrusion, and a mandible prognathism[] CADASIL NGS panel HTRA1, NOTCH3 Del Dup NGS Caffey disease COL1A1 Del Dup NGS Campomelic dysplasia SOX9 Del Dup NGS Camptodactyly, tall stature, and hearing loss syndrome[]

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